Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AUX9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006265 | DNA topological change | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0071103 | DNA conformation change | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003916 | DNA topoisomerase activity | 3 | 12 |
GO:0003917 | DNA topoisomerase type I (single strand cut, ATP-independent) activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.453 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.418 |
CLV_C14_Caspase3-7 | 728 | 732 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 751 | 753 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 799 | 801 | PF00675 | 0.640 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.177 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 799 | 801 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 698 | 700 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 720 | 722 | PF00082 | 0.519 |
CLV_PCSK_PC7_1 | 379 | 385 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.405 |
DEG_MDM2_SWIB_1 | 96 | 103 | PF02201 | 0.528 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.584 |
DEG_SCF_FBW7_2 | 500 | 505 | PF00400 | 0.154 |
DEG_SPOP_SBC_1 | 763 | 767 | PF00917 | 0.613 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.273 |
DOC_CKS1_1 | 433 | 438 | PF01111 | 0.244 |
DOC_CYCLIN_RxL_1 | 378 | 390 | PF00134 | 0.365 |
DOC_CYCLIN_RxL_1 | 684 | 697 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 148 | 156 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 261 | 269 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 3 | 14 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 445 | 451 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 457 | 465 | PF00069 | 0.232 |
DOC_MAPK_gen_1 | 545 | 551 | PF00069 | 0.422 |
DOC_MAPK_HePTP_8 | 146 | 158 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 148 | 156 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 220 | 228 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 445 | 453 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.348 |
DOC_MAPK_MEF2A_6 | 560 | 567 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 65 | 72 | PF00149 | 0.442 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.430 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 763 | 767 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 792 | 796 | PF12436 | 0.726 |
DOC_USP7_UBL2_3 | 806 | 810 | PF12436 | 0.755 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.273 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.185 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.322 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 704 | 709 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 261 | 269 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 445 | 450 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 583 | 588 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 597 | 603 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 621 | 625 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 690 | 695 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 699 | 708 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 721 | 730 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 737 | 746 | PF00244 | 0.418 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.410 |
LIG_Clathr_ClatBox_1 | 12 | 16 | PF01394 | 0.430 |
LIG_CSL_BTD_1 | 70 | 73 | PF09270 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 36 | 39 | PF00928 | 0.430 |
LIG_deltaCOP1_diTrp_1 | 486 | 493 | PF00928 | 0.289 |
LIG_EH1_1 | 321 | 329 | PF00400 | 0.365 |
LIG_EVH1_2 | 318 | 322 | PF00568 | 0.289 |
LIG_EVH1_2 | 563 | 567 | PF00568 | 0.383 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.452 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.273 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.290 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.354 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.312 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.281 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.471 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.438 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.289 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.461 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.528 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.319 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.491 |
LIG_LIR_Apic_2 | 651 | 655 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 372 | 380 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 738 | 746 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 585 | 590 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 623 | 627 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 670 | 675 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 735 | 739 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.442 |
LIG_LYPXL_yS_3 | 587 | 590 | PF13949 | 0.273 |
LIG_PCNA_PIPBox_1 | 196 | 205 | PF02747 | 0.289 |
LIG_PCNA_PIPBox_1 | 743 | 752 | PF02747 | 0.375 |
LIG_PCNA_yPIPBox_3 | 106 | 116 | PF02747 | 0.455 |
LIG_PCNA_yPIPBox_3 | 737 | 750 | PF02747 | 0.384 |
LIG_Pex14_1 | 489 | 493 | PF04695 | 0.289 |
LIG_Pex14_2 | 632 | 636 | PF04695 | 0.273 |
LIG_Pex14_2 | 668 | 672 | PF04695 | 0.323 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.528 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.410 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.289 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.308 |
LIG_SH2_GRB2like | 210 | 213 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 184 | 188 | PF00017 | 0.308 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.410 |
LIG_SH2_PTP2 | 599 | 602 | PF00017 | 0.273 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.419 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 749 | 752 | PF00017 | 0.408 |
LIG_SH3_1 | 560 | 566 | PF00018 | 0.290 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.430 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.273 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.310 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.252 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.410 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.284 |
LIG_SH3_3 | 515 | 521 | PF00018 | 0.337 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.273 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.124 |
LIG_SH3_3 | 702 | 708 | PF00018 | 0.508 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 10 | 17 | PF11976 | 0.293 |
LIG_SUMO_SIM_anti_2 | 458 | 465 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 10 | 17 | PF11976 | 0.278 |
LIG_SUMO_SIM_par_1 | 225 | 231 | PF11976 | 0.273 |
LIG_TRAF2_1 | 174 | 177 | PF00917 | 0.403 |
LIG_TRAF2_1 | 426 | 429 | PF00917 | 0.383 |
LIG_UBA3_1 | 453 | 457 | PF00899 | 0.344 |
LIG_UBA3_1 | 572 | 577 | PF00899 | 0.289 |
LIG_WRC_WIRS_1 | 665 | 670 | PF05994 | 0.328 |
LIG_WRC_WIRS_1 | 736 | 741 | PF05994 | 0.506 |
LIG_WRC_WIRS_1 | 93 | 98 | PF05994 | 0.528 |
LIG_WW_2 | 563 | 566 | PF00397 | 0.333 |
MOD_CDC14_SPxK_1 | 17 | 20 | PF00782 | 0.430 |
MOD_CDK_SPK_2 | 794 | 799 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 14 | 20 | PF00069 | 0.430 |
MOD_CDK_SPxK_1 | 267 | 273 | PF00069 | 0.230 |
MOD_CDK_SPxK_1 | 432 | 438 | PF00069 | 0.244 |
MOD_CDK_SPxK_1 | 794 | 800 | PF00069 | 0.607 |
MOD_CDK_SPxxK_3 | 267 | 274 | PF00069 | 0.410 |
MOD_CDK_SPxxK_3 | 303 | 310 | PF00069 | 0.352 |
MOD_CDK_SPxxK_3 | 313 | 320 | PF00069 | 0.284 |
MOD_CDK_SPxxK_3 | 607 | 614 | PF00069 | 0.289 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.455 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.336 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.300 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.219 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.332 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.410 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.417 |
MOD_CK1_1 | 735 | 741 | PF00069 | 0.425 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.659 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.477 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.718 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.373 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.334 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.528 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.338 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.455 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.383 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.631 |
MOD_Cter_Amidation | 104 | 107 | PF01082 | 0.258 |
MOD_Cter_Amidation | 271 | 274 | PF01082 | 0.154 |
MOD_Cter_Amidation | 381 | 384 | PF01082 | 0.388 |
MOD_DYRK1A_RPxSP_1 | 220 | 224 | PF00069 | 0.273 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.377 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.379 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.362 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.459 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.502 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.449 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.610 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.587 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.245 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.381 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.385 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.286 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.509 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.220 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.273 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.365 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.361 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.290 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.326 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.426 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.503 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.613 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.709 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.603 |
MOD_LATS_1 | 259 | 265 | PF00433 | 0.185 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.232 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.154 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.441 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.273 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.383 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.526 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.464 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.351 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.282 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.479 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.535 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.292 |
MOD_PIKK_1 | 721 | 727 | PF00454 | 0.447 |
MOD_PK_1 | 419 | 425 | PF00069 | 0.244 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.185 |
MOD_PKA_1 | 398 | 404 | PF00069 | 0.267 |
MOD_PKA_1 | 445 | 451 | PF00069 | 0.320 |
MOD_PKA_1 | 545 | 551 | PF00069 | 0.396 |
MOD_PKA_1 | 783 | 789 | PF00069 | 0.679 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.415 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.339 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.273 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.353 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.312 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.273 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.410 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.590 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.435 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.289 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.383 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.490 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.346 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.273 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.351 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.365 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.402 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.276 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.289 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.317 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.430 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.273 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.410 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.348 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.314 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.185 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.322 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.327 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.289 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.470 |
MOD_ProDKin_1 | 704 | 710 | PF00069 | 0.534 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.643 |
MOD_SUMO_for_1 | 22 | 25 | PF00179 | 0.442 |
MOD_SUMO_for_1 | 456 | 459 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 113 | 120 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 231 | 236 | PF00179 | 0.288 |
MOD_SUMO_rev_2 | 25 | 34 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 522 | 531 | PF00179 | 0.376 |
MOD_SUMO_rev_2 | 634 | 640 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 716 | 722 | PF00179 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 381 | 386 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 736 | 739 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.185 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 444 | 446 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 750 | 752 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 798 | 800 | PF00400 | 0.706 |
TRG_ER_diLys_1 | 806 | 810 | PF00400 | 0.640 |
TRG_NLS_Bipartite_1 | 795 | 810 | PF00514 | 0.645 |
TRG_NLS_MonoCore_2 | 805 | 810 | PF00514 | 0.727 |
TRG_NLS_MonoExtC_3 | 805 | 810 | PF00514 | 0.696 |
TRG_NLS_MonoExtN_4 | 804 | 810 | PF00514 | 0.646 |
TRG_Pf-PMV_PEXEL_1 | 106 | 110 | PF00026 | 0.242 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 614 | 618 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 690 | 695 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0P1 | Leptomonas seymouri | 24% | 94% |
A0A0N1PDE4 | Leptomonas seymouri | 68% | 94% |
A0A0S4J933 | Bodo saltans | 22% | 92% |
A0A0S4JDQ6 | Bodo saltans | 37% | 99% |
A0A1X0NXB2 | Trypanosomatidae | 51% | 95% |
A0A3S7WW83 | Leishmania donovani | 94% | 100% |
A0A3S7X1K1 | Leishmania donovani | 23% | 93% |
A0A422N774 | Trypanosoma rangeli | 51% | 97% |
A0R5D9 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 27% | 87% |
A0R979 | Bacillus thuringiensis (strain Al Hakam) | 25% | 100% |
A4HBL0 | Leishmania braziliensis | 86% | 99% |
A4HGN1 | Leishmania braziliensis | 23% | 100% |
A4HPI6 | Leishmania braziliensis | 22% | 85% |
A4HZ99 | Leishmania infantum | 94% | 100% |
A4I3Q5 | Leishmania infantum | 23% | 93% |
D0A1K4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AZZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 94% |
O27661 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 25% | 100% |
O28469 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 26% | 100% |
O34204 | Fervidobacterium islandicum | 25% | 100% |
O58356 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 23% | 100% |
O67226 | Aquifex aeolicus (strain VF5) | 26% | 70% |
O69548 | Mycobacterium leprae (strain TN) | 27% | 86% |
P06612 | Escherichia coli (strain K12) | 26% | 94% |
P0A2I1 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 26% | 94% |
P0A2I2 | Salmonella typhi | 26% | 94% |
P0A621 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 28% | 87% |
P0C2W6 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 21% | 100% |
P14294 | Escherichia coli (strain K12) | 21% | 100% |
P34184 | Alkalihalophilus pseudofirmus (strain ATCC BAA-2126 / JCM 17055 / OF4) | 23% | 100% |
P39814 | Bacillus subtilis (strain 168) | 27% | 100% |
P43012 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 25% | 93% |
P43704 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 21% | 100% |
P46799 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 26% | 100% |
P47368 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 24% | 100% |
P55991 | Helicobacter pylori (strain ATCC 700392 / 26695) | 26% | 100% |
P57371 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 24% | 94% |
P73810 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 28% | 90% |
P78032 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 25% | 100% |
P95479 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 24% | 67% |
P9WG48 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 28% | 87% |
P9WG49 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 28% | 87% |
Q06AK7 | Staphylococcus aureus | 25% | 100% |
Q1RIM1 | Rickettsia bellii (strain RML369-C) | 25% | 100% |
Q2FEN5 | Staphylococcus aureus (strain USA300) | 21% | 100% |
Q2FHI8 | Staphylococcus aureus (strain USA300) | 25% | 100% |
Q2FW03 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 21% | 100% |
Q2FZ32 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 25% | 100% |
Q4L8B8 | Staphylococcus haemolyticus (strain JCSC1435) | 21% | 100% |
Q4Q888 | Leishmania major | 23% | 94% |
Q4QCK3 | Leishmania major | 94% | 100% |
Q4UM42 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 26% | 100% |
Q59046 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 23% | 100% |
Q5HDV4 | Staphylococcus aureus (strain COL) | 21% | 100% |
Q5HGI2 | Staphylococcus aureus (strain COL) | 25% | 100% |
Q5HLZ4 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 21% | 100% |
Q5UQB5 | Acanthamoeba polyphaga mimivirus | 23% | 95% |
Q5WAX6 | Alkalihalobacillus clausii (strain KSM-K16) | 23% | 100% |
Q63GK5 | Bacillus cereus (strain ZK / E33L) | 25% | 100% |
Q68X45 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 25% | 100% |
Q6G767 | Staphylococcus aureus (strain MSSA476) | 21% | 100% |
Q6G9W3 | Staphylococcus aureus (strain MSSA476) | 25% | 100% |
Q6GEH9 | Staphylococcus aureus (strain MRSA252) | 21% | 100% |
Q6GHI5 | Staphylococcus aureus (strain MRSA252) | 25% | 100% |
Q6HP19 | Bacillus thuringiensis subsp. konkukian (strain 97-27) | 25% | 100% |
Q73E74 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 26% | 100% |
Q7A075 | Staphylococcus aureus (strain MW2) | 21% | 100% |
Q7A455 | Staphylococcus aureus (strain N315) | 21% | 100% |
Q7A5Y5 | Staphylococcus aureus (strain N315) | 25% | 100% |
Q81IH1 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 26% | 100% |
Q81Z97 | Bacillus anthracis | 25% | 100% |
Q87AQ6 | Xylella fastidiosa (strain Temecula1 / ATCC 700964) | 28% | 99% |
Q8CRF7 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 21% | 100% |
Q8K9P7 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 25% | 95% |
Q8NWZ9 | Staphylococcus aureus (strain MW2) | 25% | 100% |
Q92IH1 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 26% | 100% |
Q97ZF5 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 25% | 69% |
Q99S17 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 21% | 100% |
Q99UM1 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 25% | 100% |
Q9CG80 | Lactococcus lactis subsp. lactis (strain IL1403) | 26% | 100% |
Q9CN30 | Pasteurella multocida (strain Pm70) | 27% | 93% |
Q9HM08 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 24% | 100% |
Q9HZJ5 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 25% | 93% |
Q9JN65 | Mycoplasma gallisepticum (strain R(low / passage 15 / clone 2)) | 25% | 100% |
Q9KQF5 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 23% | 100% |
Q9KRB2 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 27% | 92% |
Q9PEV8 | Xylella fastidiosa (strain 9a5c) | 28% | 99% |
Q9PHK2 | Xylella fastidiosa (strain 9a5c) | 26% | 100% |
Q9PLZ2 | Campylobacter jejuni subsp. jejuni serotype O:2 (strain ATCC 700819 / NCTC 11168) | 26% | 100% |
Q9UYS8 | Pyrococcus abyssi (strain GE5 / Orsay) | 23% | 100% |
Q9X3X7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 28% | 67% |
Q9YB01 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 22% | 100% |
Q9YC75 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 25% | 67% |
Q9ZDK2 | Rickettsia prowazekii (strain Madrid E) | 25% | 100% |
Q9ZMV7 | Helicobacter pylori (strain J99 / ATCC 700824) | 26% | 100% |
V5BG04 | Trypanosoma cruzi | 53% | 99% |